Hemifacial Spasm Caused by Vascular Compression in the Cisternal Portion of the Facial Nerve: Report of Two Cases with Review of the Literature

Son, Byung-chul; Ko, Hak-cheol; Choi, Jin-gyu

doi:https://doi.org/10.1155/2019/8526157

Case Reports in Neurological Medicine

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Case Report | Open Access

Volume 2019 | Article ID 8526157 | https://doi.org/10.1155/2019/8526157

Hemifacial Spasm Caused by Vascular Compression in the Cisternal Portion of the Facial Nerve: Report of Two Cases with Review of the Literature

Byung-chul Son,^1,2Hak-cheol Ko,³and Jin-gyu Choi⁴

Academic Editor: Chin-Chang Huang

Received23 Jun 2018

Revised18 Nov 2018

Accepted13 Dec 2018

Published01 Jan 2019

Abstract

Although primary hemifacial spasm (HFS) is mostly related to a vascular compression of the facial nerve at its root exit zone (REZ), its occurrence in association with distal, cisternal portion has been repeatedly reported during the last two decades. We report two patients with typical HFS caused by distal neurovascular compression, in which the spasm was successfully treated with microvascular decompression (MVD). Vascular compression of distal, cisternal portion of the facial nerve was identified preoperatively in the magnetic resonance imaging (MRI). It was confirmed again with intraoperative findings of compression of cisternal portion of the facial nerve by the meatal loop of the anterior inferior cerebellar artery (AICA) and absence of any offending vessel in the REZ of the facial nerve. Immediate disappearance of lateral spread response (LSR) after decompression and resolution of spasm after the operation again validated that HFS in the current patients originated from the vascular compression of distal, cisternal portion of the facial nerves. According to our literature review of 64 patients with HFS caused by distal neurovascular compression, distal compression can be classified by pure distal neurovascular compression (31 cases, 48.4%) and double compression (both distal segment and the REZ of the facial nerves, 33 cases [51.6%]) according to the presence or absence of simultaneous offender in the REZ. Eighty-four percent of 64 identified distal offenders were the AICA, especially its meatal and postmeatal segments. Before awareness of distal neurovascular compression causing HFS and sophisticated MRI imaging (before 2000), the rate of reoperation was high (58%). Preoperative MRI and intraoperative monitoring of LSR seems to be an essential element in determination of real offending vessel in MVD caused by distal offender.

1. Introduction

Primary HFS is generally regarded as the result of hyperexcitability of the facial nerve and its nucleus caused by vascular compression of the facial nerve at its root exit zone (REZ) [1–13]. However, HFS caused by vascular compression in the distal portions of the facial nerve has been sporadically reported [14–23]. In the reports of HFS caused by vascular compression of the distal, cisternal portion of the facial nerve, distal neurovascular compression has mostly been identified by intraoperative finding during repeated MVD for recurrences or failures after MVD [9, 15–17]. However, preoperative identification of distal neurovascular conflict is now increasing since introduction of sophisticated MRI examination in HFS [18, 19, 24–26].

We report two patients with typical HFS caused by pure cisternal neurovascular compression of the facial nerve by the meatal and postmeatal segments of the AICAs. We summarized a detailed review of literature regarding HFS caused by distal neurovascular compression according to the pattern of the offending vessels. According to literature review of HFS caused by distal neurovascular compression, distal neurovascular compression can be classified by pure neurovascular compression in distal, cisternal portion by a single artery (mostly by the anterior inferior cerebellar artery [AICA]) and double compression (both REZ and the distal portion) by a single arterial loop or two different offending arteries (e.g., AICA and the posterior inferior cerebellar artery [PICA], or AICA and the vertebral artery [VA]).

In determination of true distal offender, intraoperative monitoring of lateral spread response (LSR) was helpful. LSR is an abnormal muscle response demonstrated by EMG recordings from mimic muscles that are innervated by a different branch of the facial nerve [3, 27–29]. When the offending vessel is moved off the REZ of the facial nerve, LSR disappears instantly in most patients [3, 22, 27–29]. Although seeking elimination of LSR in all patients after verification of complete decompression is not recommended [30], assuring disappearance of LSR could enhance surgical success rate without missing possible hidden offenders around the REZ. Although importance of LSR monitoring during primary and repeated MVDs has been reported [11, 12, 27–29, 31–33], its role in determination of distal offender has been rarely addressed [19].

2. Case Report

2.1. Case 1

A 50-year-old male patient presented with a 2-year history of left-sided typical HFS. Painless irregular clonic contraction of the facial muscles began initially in the orbicularis oculi muscle of the lower lid. It gradually spread to other muscles innervated by the facial nerve on the left side of the face, including platysma. The paroxysm was induced or aggravated by emotional tension, stress, and voluntary and reflexive movements of the face. He had significant difficulty in his work and social life despite 2 times of botulinum toxin injection. Medical treatment with carbamazepine (up to 600 mg) and baclofen (30 mg) was not effective. He was referred for surgical treatment. His medical history was unremarkable. His physical and neurologic examinations were normal, including hearing. No tinnitus or discernible noise heard in his left ear was found. Only typical nature of clonic hemifacial spasm was evident. Abnormal synkinesis between the orbicularis oculi and orbicularis oris muscles was found by the electromyographic examination of the blink reflex. Despite typical HFS, there was no discernible vascular structure in the REZ of left facial nerve (Figure 1(a)). However, a meatal loop of AICA abutting to the cisternal portion of the facial nerve was found.

(a) In the axial CISS image of left cerebellopontine angle, there was no vascular structure in the REZ of the facial nerve (arrowhead). A meatal loop of the anterior inferior cerebellar artery (AICA) is in close approximation with the cisternal portion of the facial nerve (arrow)

(b) An intraoperative photography showing an absence of any vascular offender in the root exit zone (REZ) of the facial nerve (arrow). Note the indentation of the distal facial nerve by the loop of the AICA (asterisk). : the seventh (facial) nerve, : the eighth (vestibulocochlear) nerve

(c) An intraoperative photography showing decompression of distal facial nerve with a small piece of Teflon felt from the loop of AICA (asterisk)

(d) Immediate disappearance of lateral spread response (LSR) of the facial EMG (mentalis muscle) following decompression of distal, cisternal portion of the facial nerve (left). Brainstem auditory evoked potential (BAEP) was stable (right)

Under the impression of HFS caused by neurovascular compression of distal facial nerve, standard microsurgical procedure was performed as described previously [5, 7, 10]. In addition to intraoperative monitoring of BAEPs, LSR, which is an abnormal muscle response demonstrated by EMG recordings from mimic muscles that are innervated by a different branch of the facial nerve [3], was also monitored throughout the operation. The entire course of the facial nerve and offending arteries were exposed under microscopic vision. Upon exposure of the REZ of the facial nerve, there was no offending vessel in the REZ as expected (Figure 1(b)). The distal, cisternal segment of the facial nerve was found to be bent by a meatal loop of the AICA (Figure 1(b)). A small piece of Teflon felt was interposed between the facial nerve and the meatal loop of the AICA with extreme care not to stretch the internal auditory artery and the distal facial nerve (Figure 1(c)). After interposition of Teflon felt, LSR immediately disappeared and BEAP was stable also (Figure 1(d)). The closure of the dura and wound was performed in routine manner. The HFS resolved completely following the surgery. The postoperative course was uneventful with no signs of facial weakness or hearing impairment by pure-tone audiometry. No recurrence of HFS or neurologic sequelae was evident at a 12-month follow-up.

2.2. Case 2

A 58-year-old female patient presented with a 1-year history of right-sided typical HFS. The nature of spasm was similar to case 1 and identified as typical HFS. It progressively worsened and did not respond to medical treatment and botulinum toxin was effective only for three months. She wanted to have a definitive treatment and transferred to our department. Her neurologic examination was normal except painless irregular clonic contraction of the facial muscles, consistent with typical HFS. In the MRI, although the PICA passed around the REZ of the facial nerve, it did not compress the REZ (Figure 2(a)). The postmeatal segment of AICA coursed between the vestibulocochlear and facial nerves. Under suspicion of HFS by distal neurovascular compression, MVD was performed with intraoperative monitoring of LSR and BAEP. As expected, the PICA had no association with the REZ or attached segment of the facial nerve (Figure 2(b)). The postmeatal segment of AICA was interposed between the vestibulocochlear and facial nerves and adhered to the distal cisternal segment of the facial nerve. It was carefully separated from the facial nerve and 2 thin leaflets of Teflon were interposed between the postmeatal AICA and the facial nerve (Figure 2(c)). Disappearance of LSR was confirmed within 2 minutes (Figure 2(d)). After awakening from anesthesia, the spasm disappeared. Postoperative course was uneventful with any facial weakness or hearing impairment by pure-tone audiometry. She discharged at the fifth postoperative day and no recurrence was found at 6 months postoperatively.

(a) An axial CISS MRI image of left cerebellopontine angle. Although the PICA (black arrowhead) is close to the REZ of the facial nerve (white arrowhead), there is no compression in the REZ (white arrowhead). The postmeatal segment of AICA (white arrow) is passing horizontally between the vestibulocochlear and facial nerves. The black arrow indicates the meatal segment of AICA

(b) An intraoperative photography showing an absence of any vascular offender in the root exit zone (REZ) of the facial nerve (arrow). There was no compression of the REZ from the loop of PICA. : the seventh (facial) nerve, : the eighth (vestibulocochlear) nerve, FL: flocculus

(c) The postmeatal segment of AICA (white arrow) is interposed between the vestibulocochlear and facial nerves. Although a small piece of Teflon (asterisk) was interposed below the loop of PICA, LSR did not disappear (Figure 2(e), black asterisk). Note the premeatal segment of AICA (arrowhead) behind the PICA

(d) After mobilization of the postmeatal segment of AICA (arrow) with dissection from the distal facial nerve, LSR disappeared (Figure 2(e), white asterisks)

(e) Disappearance of LSR of the facial EMG (orbicularis oculi muscle) following decompression of distal facial nerve (white asterisks) from the postmeatal segment of AICA. Teflon insertion beneath the PICA did not affect the LSR (black asterisk)

3. Discussion

3.1. Primary Hemifacial Spasm Caused by Distal Offender and Its Preoperative Identification

According to our literature review (Table 1), the problems associated with MVD for primary HFS caused by distal neurovascular compression are preoperative identification of distal compression and high rate of reoperation. In the period (1990s and early 2000s) when a detailed MRI examination and intraoperative monitoring of LSR were not popular, distal neurovascular compression was confirmed only during the repeated operation for spasm recurrence or surgical failure [15], or an intraoperative finding of only distal offender with its absence in the REZ [14, 16, 17]. Indeed, 7 (58%) of the 12 reported cases of distal neurovascular compression before 2000 needed a reexploration to figure out the presence of distal compression [14–17]. The description of the outcome of the first MVDs on HFS with distal offenders was often vague, without distinguishing persistence or recurrence of HFS. Recurrence represents symptoms reappearing postoperatively after a symptom-free interval of more than 1 year [34]. When there is no improvement or worsening of symptoms after one year postoperatively, it is called “incomplete cure” or persistence [34, 35]. Reasons for an unsuccessful MVD include incomplete decompression by not identifying the true culprit vessels, presence of a previously unidentified secondary offending vessel, or implant compression/migration against the facial nerve [36–38].

In addition, LSR monitoring was not performed in all 12 cases of distal neurovascular compression reported before 2000 [14–17]. Lack of knowledge about the utility of LSR monitoring during MVD in that era might have resulted in a high rate of failure and recurrence (58%) in HFS caused by distal offenders. Although true value of LSR monitoring is still in doubt, a meta-analysis study found that the chance of a cure if LSR was abolished during surgery was 4.2 times greater than that if LSR persisted [11]. Because the reports specifically addressing HFS associated with distal offenders are rare, the results of LSR monitoring in this situation are largely unknown.

Sophisticated MRI techniques for lower cranial nerves in the cerebellopontine angle and the internal auditory canal were introduced in late 1990s and were popularized since early 2000s [24, 39]. The three-dimensional constructive interference of steady-state sequence (3D CISS) and three-dimensional fast imaging employing steady-state acquisition (3D FIESTA) technique [24, 26, 39, 40] provided superior visualization of neurovascular relationships with the excellent CSF-nerve contrast and high spatial resolution. They have enabled preoperative identification of HFS caused by distal neurovascular compression [18, 19, 24–26]. However, even with well-visualization of the neurovascular structures in and around the REZ and distal facial nerve, there are many asymptomatic neurovascular contacts in the facial nerve [19, 24–27, 41]. Multiple offenders are also common [19, 23, 27]. Multiple compression by a single artery, such as compression of the REZ by premeatal segment of the AICA and distal compression by its distal meatal segment, has also been reported [23]. Therefore, unless there is no definite arterial offender in the REZ in patients with typical HFS associated with only single, suspicious offending vessel in the distal facial nerve, it is difficult to make a preoperative diagnose of HFS caused by distal neurovascular conflict. Furthermore, HFS associated with venous offender was also reported [42–44].

In our review of distal neurovascular compression causing HFS, it was found to occur in 2 types according to the presence or absence of additional vascular offenders in the REZ. Therefore, it can be assorted into the pattern of distal compression: (1) pure distal compression by single offender without any offender in the REZ (PDC type), (2) double compression in both distal cisternal portion and the REZ of the facial nerve (DC type). A total of 64 cases of surgically proven patients with HFS caused by distal compression were identified, including current 2 cases (Table 1). Thirty-one cases (48.4%) were found to be PDC type and 33 cases (51.6%) were DC type. The incidence of distal neurovascular compression varied significantly according to the reports, ranging from 5.9% to 1 out of 753 patients [9, 22, 23].

With development of new techniques of MRI examinations and spread of knowledge regarding distal neurovascular compression in HFS, rate of reoperation in distal compression decreased significantly since 2000. Among 52 reported cases of distal compression after 2000, 1 of 25 PDCs (4%) and 7 (25.9%) of 27 DCs needed repeated operations. However, the rate of reoperation in DC type is high and still poses significant problem during MVD for HFS [12, 22, 23]. Difficulty in determination of real culprit offender in the presence of double compression in both distal segment and the REZ of the facial nerve (DC type) during the microsurgical operation has been repeatedly stressed by several authors [12, 15, 22, 23]. Furthermore, importance of awareness of DC type was suggested as early as 1991 by Nagahiro et al. [15] as “sandwich type”. Zheng et al. [23] stressed it as “cross-type” compression again. Although the uncertainty associated with HFS caused by PDC type decreased significantly with preoperative identification and intraoperative LSR monitoring as shown in the current 2 cases, it seems that those with DC type still pose significant surgical challenges during MVD.

3.2. Meatal and Postmeatal Segments of the Anterior Inferior Cerebellar Artery (AICA) as Distal Offender

Fifty-four (84.3%) identified distal offenders among 64 cases of HFS caused by distal compression were the AICA and seven (10.9%) were the PICA. Since the early reports by Yeh et al. [14] and Nagahiro et al. [15], the AICA was the main distal offender causing HFS. Among the four segments (anterior pontine, lateral pontine, flocculonodular, and cortical) of the AICA [45], the second (lateral pontine) segment gives rise to the nerve-related branches that course near or within the internal acoustic meatus in close relationship to the facial and vestibulocochlear nerves. This segment is divided into premeatal, meatal, and postmeatal parts, depending on their relationship to the porus acusticus. The premeatal segment of the AICA courses around the brainstem to reach the facial and vestibulocochlear nerves and the anterior edge of the meatus. Most (46 of the 56, 82%) of the premeatal segments were anteroinferior to the nerves and, therefore, they are common offenders in the REZ of the facial nerve [45]. The meatal segment, located in the vicinity of the internal acoustic meatus, often forms a laterally convex loop directed toward the meatus. The majority of the meatal loops coursed in a horizontal plane above or below the nerves, but some, mostly those passing between the facial and vestibulocochlear nerves, course in a vertical or oblique plane [45]. These meatal and postmeatal segments of the AICA passing between the facial and vestibulocochlear nerves, as shown in current report, have been repeatedly identified and described as “interposed AICA between the facial and vestibulocochlear nerves” [12, 14–19, 22].

3.3. Role of Lateral Spread Response during MVD for HFS Caused by Distal Offender

When there is a single offending artery in the distal segment of the facial nerve (PDC type) and LSR is consistent after exposure of the REZ of the facial nerve during MVD, it can be a reliable means of confirming the culprit vessel. Even if there are dual offending vessels along the facial nerve, both in the REZ and distal segment (DC type), LSR may be a reliable indicator of adequate decompression [31–33]. If LSR disappears immediately after initial decompression of the REZ, further decompression of distal facial nerve may not be needed. However, if LSR persists despite adequate decompression, deciding to perform distal decompression is difficult and is at the surgeon’s discretion.

4. Conclusions

Two cases of typical HFS caused by distal neurovascular compression of the meatal and postmeatal segments of AICA are presented. According to literature review, HFS caused by distal neurovascular compression could be classified into a pure distal compression (PDC type) and those with double compression in both the REZ and distal segment of the facial nerves (DC type). The meatal and postmeatal segments of AICA are the most common distal offenders. Preoperative suspicion of distal compression with MRI examination and intraoperative verification of distal offender in absence of offenders in the REZ of the facial nerve, combined with intraoperative monitoring of LSR, seems to be essential element in MVD for HFS caused by distal offenders.

Ethical Approval

All procedures performed in this study involving human participants were in accordance with ethical standards of the Institutional and/or National Research Committee and the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Conflicts of Interest

The authors declare that they have no conflicts of interest regarding this manuscript.

References

P. J. Jannetta, “The cause of hemifacial spasm: definitive microsurgical treatment at the brainstem in 31 patients,” Transactions of the American Academy of Ophthalmology and Otolaryngology, vol. 80, pp. 319–322, 1975.
View at: Google Scholar
P. J. Jannetta, M. Abbasy, J. C. Maroon, F. M. Ramos, and M. S. Albin, “Etiology and definitive microsurgical treatment of hemifacial spasm. Operative techniques and results in 47 patients,” Journal of Neurosurgery, vol. 47, no. 3, pp. 321–328, 1977.
View at: Publisher Site | Google Scholar
A. R. Moller and P. J. Jannetta, “Microvascular decompression in hemifacial spasm: Intraoperative electrophysiological observations,” Neurosurgery, vol. 16, no. 5, pp. 612–618, 1985.
View at: Publisher Site | Google Scholar
A. Kondo, “Follow-up results of microvascular decompression in trigeminal neuralgia and hemifacial spasm,” Neurosurgery, vol. 40, no. 1, pp. 46–52, 1997.
View at: Publisher Site | Google Scholar
M. R. McLaughlin, P. J. Jannetta, B. L. Clyde, B. R. Subach, C. H. Comey, and D. K. Resnick, “Microvascular decompression of cranial nerves: lessons learned after 4400 operations,” Journal of Neurosurgery, vol. 90, no. 1, pp. 1–8, 1999.
View at: Publisher Site | Google Scholar
M. Samii, T. Günther, G. Iaconetta et al., “Microvascular decompression to treat hemifacial spasm: Long-term results for a consecutive series of 143 patients,” Neurosurgery, vol. 50, no. 4, pp. 712–719, 2002.
View at: Publisher Site | Google Scholar
T. Hitotsumatsu, T. Matsushima, T. Inoue et al., “Microvascular Decompression for Treatment of Trigeminal Neuralgia, Hemifacial Spasm, and Glossopharyngeal Neuralgia: Three Surgical Approach Variations: Technical Note,” Neurosurgery, vol. 53, no. 6, pp. 1436–1443, 2003.
View at: Publisher Site | Google Scholar
M. P. Sindou, “Microvascular decompression for primary hemifacial spasm. Importance of intraoperative neurophysiological monitoring,” Acta Neurochirurgica, vol. 147, no. 10, pp. 1019–1026, 2005.
View at: Publisher Site | Google Scholar
M. Campos-Benitez and A. M. Kaufmann, “Neurovascular compression findings in hemifacial spasm,” Journal of Neurosurgery, vol. 109, no. 3, pp. 416–420, 2008.
View at: Publisher Site | Google Scholar
J. S. Park, D. S. Kong, J. A. Lee, and K. Park, “Hemifacial spasm: neurovascular compressive patterns and surgical significance,” Acta Neurochirurgica, vol. 150, no. 3, pp. 235–241, 2008.
View at: Publisher Site | Google Scholar
R. F. Sekula Jr., S. Bhatia, A. M. Frederickson et al., “Utility of intraoperative electromyography in microvascular decompression for hemifacial spasm: a meta-analysis,” Neurosurgical Focus, vol. 27, no. 4, pp. E10.1–E10.6, 2009.
View at: Publisher Site | Google Scholar
J. Zhong, J. Zhu, S. Li et al., “An analysis of failed microvascular decompression in patients with hemifacial spasm: focused on the early reoperative findings,” Acta Neurochirurgica, vol. 152, no. 12, pp. 2119–2123, 2010.
View at: Publisher Site | Google Scholar
A. Fukunaga, K. Shimizu, T. Yazaki, and M. Ochiai, “A recommendation on the basis of long-term follow-up resultsof our microvascular decompression operation for hemifacial spasm,” Acta Neurochirurgica, vol. 155, no. 9, pp. 1693–1697, 2013.
View at: Publisher Site | Google Scholar
H. S. Yeh, J. M. Tew Jr., and R. M. Ramirez, “Microsurgical treatment of intractable hemifacial spasm,” Neurosurgery, vol. 9, no. 4, pp. 383–386, 1981.
View at: Publisher Site | Google Scholar
S. Nagahiro, A. Takada, Y. Matsukado, and Y. Ushio, “Microvascular decompression for hemifacial spasm. Patterns of vascular compression in unsuccessfully operated patients,” Journal of Neurosurgery, vol. 75, no. 3, pp. 388–392, 1991.
View at: Publisher Site | Google Scholar
M. Fukuda, S. Kameyama, Y. Honda, and R. Tanaka, “Hemi facial Spasm Resulting from Facial Nerve Compression Near the Internal Acoustic Meatus - Case Report,” Neurologia Medico-Chirurgica, vol. 37, no. 10, pp. 771–774, 1997.
View at: Publisher Site | Google Scholar
H. Ryu, S. Yamamoto, K. Sugiyama, K. Uemura, and T. Miyamoto, “Hemifacial spasm caused by vascular compression of the distal portion of the facial nerve: Report of seven cases,” Journal of Neurosurgery, vol. 88, no. 3, pp. 605–609, 1998.
View at: Publisher Site | Google Scholar
K. Onoda, K. Tokunaga, Y. Miyoshi, S. Ono, and I. Date, “Hemifacial spasm due to vascular compression of the distal portion of root exit zone of the facial nerve: Report of two cases,” Journal of Neurological Surgery, vol. 34, no. 4, pp. 397–400, 2006.
View at: Google Scholar
M. Kawashima, M. Yamada, S. Sato, H. Oka, K. Fujii, and T. Matsushima, “Hemifacial spasm caused by vascular compression of the distal portion of the facial nerve associated with configuration variation of the facial and vestibulocochlear nerve complex,” Turkish Neurosurgery, vol. 19, no. 3, pp. 269–275, 2009.
View at: Google Scholar
W. S. Chang, H. Y. Kim, S. S. Chung, and J. W. Chang, “Microneurovascular decompression in patients with hemifacial spasm caused by vascular compression of facial nerve at cisternal portion,” Acta Neurochirurgica, vol. 152, no. 12, pp. 2105–2111, 2010.
View at: Publisher Site | Google Scholar
J. Zhong, S.-T. Li, J. Zhu, and H.-X. Guan, “Is entire nerve root decompression necessary for hemifacial spasm?” International Journal of Surgery, vol. 9, no. 3, pp. 254–257, 2011.
View at: Publisher Site | Google Scholar
S. Li, W. Hong, Y. Tang et al., “Re-operation for persistent hemifacial spasm after microvascular decompression with the aid of intraoperative monitoring of abnormal muscle response,” Acta Neurochirurgica, vol. 152, no. 12, pp. 2113–2117, 2010.
View at: Publisher Site | Google Scholar
X. Zheng, B. Feng, W. Zhang, T. Ying, and S. Li, “Hemifacial spasm caused by cross type vascular compression,” Neurological Research, vol. 33, no. 9, pp. 965–969, 2011.
View at: Publisher Site | Google Scholar
I. Yousry, S. Camelio, U. D. Schmid et al., “Visualization of cranial nerves I-XII: Value of 3D CISS and T2-weighted FSE sequences,” European Radiology, vol. 10, no. 7, pp. 1061–1067, 2000.
View at: Publisher Site | Google Scholar
M. Sindou, “Trigeminal neuralgia: A plea for microvascular decompression as the first surgical option. Anatomy should prevail,” Acta Neurochirurgica, vol. 152, no. 2, pp. 361–364, 2010.
View at: Publisher Site | Google Scholar
I. Yamakami, E. Kobayashi, S. Hirai et al., “Preoperative assessment of trigeminal neuralgia and hemifacial spasm using constructive interference in steady state-three-dimensional fourier transformation magnetic resonance imaging,” Neurologia medico-chirurgica, vol. 40, no. 11, pp. 545–556, 2000.
View at: Publisher Site | Google Scholar
B. C. Son, H. C. Ko, and J. G. Choi, “Intraoperative monitoring of Z-L response (ZLR) and abnormal muscle response (AMR) during microvascular decompression for hemifacial spasm. Interpreting the role of ZLR,” Acta Neurochirurgica, vol. 160, pp. 963–970, 2018.
View at: Google Scholar
A. R. Møller, “Vascular compression of cranial nerves: II: Pathophysiology,” Neurological Research, vol. 21, no. 5, pp. 439–443, 1999.
View at: Publisher Site | Google Scholar
I. Fernández-Conejero, S. Ulkatan, C. Sen, and V. Deletis, “Intra-operative neurophysiology during microvascular decompression for hemifacial spasm,” Clinical Neurophysiology, vol. 123, no. 1, pp. 78–83, 2012.
View at: Publisher Site | Google Scholar
Y. Wei, W. Yang, W. Zhao et al., “Microvascular decompression for hemifacial spasm: Can intraoperative lateral spread response monitoring improve surgical efficacy?” Journal of Neurosurgery, vol. 128, no. 3, pp. 885–890, 2018.
View at: Publisher Site | Google Scholar
S.-J. Hyun, D.-S. Kong, and K. Park, “Microvascular decompression for treating hemifacial spasm: Lessons learned from a prospective study of 1,174 operations,” Neurosurgical Review, vol. 33, no. 3, pp. 325–334, 2010.
View at: Publisher Site | Google Scholar
T.-T. Ying, S.-T. Li, J. Zhong, X.-Y. Li, X.-H. Wang, and J. Zhu, “The value of abnormal muscle response monitoring during microvascular decompression surgery for hemifacial spasm,” International Journal of Surgery, vol. 9, no. 4, pp. 347–351, 2011.
View at: Publisher Site | Google Scholar
P. D. Thirumala, X. Wang, A. Shah et al., “Clinical impact of residual lateral spread response after adequate microvascular decompression for hemifacial spasm: A retrospective analysis,” British Journal of Neurosurgery, vol. 29, no. 6, pp. 818–822, 2015.
View at: Publisher Site | Google Scholar
A. Kondo, I. Date, S. Endo et al., “A proposal for standardized analysis of the results of microvascular decompression for trigeminal neuralgia and hemifacial spasm,” Acta Neurochirurgica, vol. 154, no. 5, pp. 773–778, 2012.
View at: Publisher Site | Google Scholar
T. Hatayama, T. Kono, Y. Harada et al., “Indications and timings of re-operation for residual or recurrent hemifacial spasm after microvascular decompression: Personal experience and literature review,” Neurologia medico-chirurgica, vol. 55, no. 8, pp. 663–668, 2015.
View at: Publisher Site | Google Scholar
X. Wang, P. D. Thirumala, A. Shah et al., “Microvascular decompression for hemifacial spasm: focus on late reoperation,” Neurosurgical Review, vol. 36, no. 4, pp. 637–643, 2013.
View at: Publisher Site | Google Scholar
M. A. Hughes, B. F. Branstetter, C. T. Taylor et al., “MRI findings in patients with a history of failed prior microvascular decompression for hemifacial spasm: How to image and where to look,” American Journal of Neuroradiology, vol. 36, no. 4, pp. 768–773, 2015.
View at: Publisher Site | Google Scholar
M. G. Bigder and A. M. Kaufmann, “Failed microvascular decompression surgery for hemifacial spasm due to persistent neurovascular compression: An analysis of reoperations,” Journal of Neurosurgery, vol. 124, no. 1, pp. 90–95, 2016.
View at: Publisher Site | Google Scholar
J. W. Casselman, R. Kuhweide, M. Deimling, W. Ampe, I. Dehaene, and L. Meeus, “Constructive interference in steady state-3DFT MR imaging of the inner ear and cerebellopontine angle,” American Journal of Neuroradiology, vol. 14, no. 1, pp. 47–57, 1993.
View at: Google Scholar
W. R. Nitz, “Fast and ultrafast non-echo-planar MR imaging techniques,” European Radiology, vol. 12, no. 12, pp. 2866–2882, 2002.
View at: Google Scholar
A. M. Raslan, R. DeJesus, C. Berk, A. Zacest, J. C. Anderson, and K. J. Burchiel, “Sensitivity of high-resolution three-dimensional magnetic resonance angiography and three-dimensional spoiled-gradient recalled imaging in the prediction of neurovascular compression in patients with hemifacial spasm: Clinical article,” Journal of Neurosurgery, vol. 111, no. 4, pp. 733–736, 2009.
View at: Publisher Site | Google Scholar
P. J. Jannetta, “Hemifacial spasm caused by a venule: Case report,” Neurosurgery, vol. 14, no. 1, pp. 89–92, 1984.
View at: Publisher Site | Google Scholar
X. Wang, P. D. Thirumala, A. Shah et al., “The role of vein in microvascular decompression for hemifacial spasm: A clinical analysis of 15 cases,” Neurological Research, vol. 35, no. 4, pp. 389–394, 2013.
View at: Publisher Site | Google Scholar
J. Eun, J. G. Choi, and B. C. Son, “Hemifacial spasm caused by a vein: a case report,” Asian Journal of Neurosurgery, vol. 13, pp. 786–788, 2018.
View at: Google Scholar
A. L. Rhoton Jr, “The cerebellar arteries,” in Cranial and Surgical Approaches, A. L. Rhoton Jr, Ed., pp. 476–483, Lippoincott, Williams & Wilkins, 2003.
View at: Google Scholar

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Copyright © 2019 Byung-chul Son et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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